author_facet Song, Dengmeng
Li, Bo
Li, Xin
Sun, Xuzhuo
Li, Jun
Li, Chengbo
Xu, Tongyu
Zhu, Yong
Li, Fei
Wang, Ning
Song, Dengmeng
Li, Bo
Li, Xin
Sun, Xuzhuo
Li, Jun
Li, Chengbo
Xu, Tongyu
Zhu, Yong
Li, Fei
Wang, Ning
author Song, Dengmeng
Li, Bo
Li, Xin
Sun, Xuzhuo
Li, Jun
Li, Chengbo
Xu, Tongyu
Zhu, Yong
Li, Fei
Wang, Ning
spellingShingle Song, Dengmeng
Li, Bo
Li, Xin
Sun, Xuzhuo
Li, Jun
Li, Chengbo
Xu, Tongyu
Zhu, Yong
Li, Fei
Wang, Ning
ChemSusChem
Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
General Energy
General Materials Science
General Chemical Engineering
Environmental Chemistry
author_sort song, dengmeng
spelling Song, Dengmeng Li, Bo Li, Xin Sun, Xuzhuo Li, Jun Li, Chengbo Xu, Tongyu Zhu, Yong Li, Fei Wang, Ning 1864-5631 1864-564X Wiley General Energy General Materials Science General Chemical Engineering Environmental Chemistry http://dx.doi.org/10.1002/cssc.201902668 <jats:title>Abstract</jats:title><jats:p>The fabrication of efficient and convenient photocatalytic H<jats:sub>2</jats:sub> evolution systems is a fascinating research topic in the field of solar energy conversion. A ternary self‐assembled photocatalytic H<jats:sub>2</jats:sub> evolution system was fabricated through supramolecular host–guest chemistry. The system consisted of the H<jats:sub>2</jats:sub> evolution catalyst [Co(dmgH)<jats:sub>2</jats:sub>(4‐ppy)<jats:sub>2</jats:sub>]NO<jats:sub>3</jats:sub> (<jats:bold>1</jats:bold>; dmgH<jats:sub>2</jats:sub>=dimethylglyoxime, 4‐ppy=4‐phenylpyridine) and the photosensitizer Eosin Y (EY) assembled with the macrocyclic compound cucurbit[7]uril (CB[7]) to form the <jats:bold>1</jats:bold>@CB[7]/EY complex through inclusion and exclusion interactions, respectively. The synchronous self‐assembly drives an orthogonal arrangement of the <jats:bold>1</jats:bold>@CB[7]/EY system. The inclusion complex <jats:bold>1</jats:bold>@CB[7] was successfully characterized by <jats:sup>1</jats:sup>H NMR spectroscopy and single‐crystal XRD. The exclusion process of CB[7] with EY was identified by NMR titration and the optimized geometry of the exclusion structure was determined by DFT calculations. The use of CB[7] resulted in a 6‐fold increase in turnover number, a 3‐fold increase in turnover frequency, and a 3‐fold extension of lifetime for photocatalytic H<jats:sub>2</jats:sub> evolution as compared with the system in the absence of CB[7]. The improvement of the light‐driven H<jats:sub>2</jats:sub> evolution activity was ascribed to the ability of CB[7] to link the photosensitizer and catalyst.</jats:p> Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H<sub>2</sub> Evolution ChemSusChem
doi_str_mv 10.1002/cssc.201902668
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series ChemSusChem
source_id 49
title Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_unstemmed Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_full Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_fullStr Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_full_unstemmed Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_short Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_sort orthogonal supramolecular assembly triggered by inclusion and exclusion interactions with cucurbit[7]uril for photocatalytic h<sub>2</sub> evolution
topic General Energy
General Materials Science
General Chemical Engineering
Environmental Chemistry
url http://dx.doi.org/10.1002/cssc.201902668
publishDate 2020
physical 394-399
description <jats:title>Abstract</jats:title><jats:p>The fabrication of efficient and convenient photocatalytic H<jats:sub>2</jats:sub> evolution systems is a fascinating research topic in the field of solar energy conversion. A ternary self‐assembled photocatalytic H<jats:sub>2</jats:sub> evolution system was fabricated through supramolecular host–guest chemistry. The system consisted of the H<jats:sub>2</jats:sub> evolution catalyst [Co(dmgH)<jats:sub>2</jats:sub>(4‐ppy)<jats:sub>2</jats:sub>]NO<jats:sub>3</jats:sub> (<jats:bold>1</jats:bold>; dmgH<jats:sub>2</jats:sub>=dimethylglyoxime, 4‐ppy=4‐phenylpyridine) and the photosensitizer Eosin Y (EY) assembled with the macrocyclic compound cucurbit[7]uril (CB[7]) to form the <jats:bold>1</jats:bold>@CB[7]/EY complex through inclusion and exclusion interactions, respectively. The synchronous self‐assembly drives an orthogonal arrangement of the <jats:bold>1</jats:bold>@CB[7]/EY system. The inclusion complex <jats:bold>1</jats:bold>@CB[7] was successfully characterized by <jats:sup>1</jats:sup>H NMR spectroscopy and single‐crystal XRD. The exclusion process of CB[7] with EY was identified by NMR titration and the optimized geometry of the exclusion structure was determined by DFT calculations. The use of CB[7] resulted in a 6‐fold increase in turnover number, a 3‐fold increase in turnover frequency, and a 3‐fold extension of lifetime for photocatalytic H<jats:sub>2</jats:sub> evolution as compared with the system in the absence of CB[7]. The improvement of the light‐driven H<jats:sub>2</jats:sub> evolution activity was ascribed to the ability of CB[7] to link the photosensitizer and catalyst.</jats:p>
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author Song, Dengmeng, Li, Bo, Li, Xin, Sun, Xuzhuo, Li, Jun, Li, Chengbo, Xu, Tongyu, Zhu, Yong, Li, Fei, Wang, Ning
author_facet Song, Dengmeng, Li, Bo, Li, Xin, Sun, Xuzhuo, Li, Jun, Li, Chengbo, Xu, Tongyu, Zhu, Yong, Li, Fei, Wang, Ning, Song, Dengmeng, Li, Bo, Li, Xin, Sun, Xuzhuo, Li, Jun, Li, Chengbo, Xu, Tongyu, Zhu, Yong, Li, Fei, Wang, Ning
author_sort song, dengmeng
container_issue 2
container_start_page 394
container_title ChemSusChem
container_volume 13
description <jats:title>Abstract</jats:title><jats:p>The fabrication of efficient and convenient photocatalytic H<jats:sub>2</jats:sub> evolution systems is a fascinating research topic in the field of solar energy conversion. A ternary self‐assembled photocatalytic H<jats:sub>2</jats:sub> evolution system was fabricated through supramolecular host–guest chemistry. The system consisted of the H<jats:sub>2</jats:sub> evolution catalyst [Co(dmgH)<jats:sub>2</jats:sub>(4‐ppy)<jats:sub>2</jats:sub>]NO<jats:sub>3</jats:sub> (<jats:bold>1</jats:bold>; dmgH<jats:sub>2</jats:sub>=dimethylglyoxime, 4‐ppy=4‐phenylpyridine) and the photosensitizer Eosin Y (EY) assembled with the macrocyclic compound cucurbit[7]uril (CB[7]) to form the <jats:bold>1</jats:bold>@CB[7]/EY complex through inclusion and exclusion interactions, respectively. The synchronous self‐assembly drives an orthogonal arrangement of the <jats:bold>1</jats:bold>@CB[7]/EY system. The inclusion complex <jats:bold>1</jats:bold>@CB[7] was successfully characterized by <jats:sup>1</jats:sup>H NMR spectroscopy and single‐crystal XRD. The exclusion process of CB[7] with EY was identified by NMR titration and the optimized geometry of the exclusion structure was determined by DFT calculations. The use of CB[7] resulted in a 6‐fold increase in turnover number, a 3‐fold increase in turnover frequency, and a 3‐fold extension of lifetime for photocatalytic H<jats:sub>2</jats:sub> evolution as compared with the system in the absence of CB[7]. The improvement of the light‐driven H<jats:sub>2</jats:sub> evolution activity was ascribed to the ability of CB[7] to link the photosensitizer and catalyst.</jats:p>
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spelling Song, Dengmeng Li, Bo Li, Xin Sun, Xuzhuo Li, Jun Li, Chengbo Xu, Tongyu Zhu, Yong Li, Fei Wang, Ning 1864-5631 1864-564X Wiley General Energy General Materials Science General Chemical Engineering Environmental Chemistry http://dx.doi.org/10.1002/cssc.201902668 <jats:title>Abstract</jats:title><jats:p>The fabrication of efficient and convenient photocatalytic H<jats:sub>2</jats:sub> evolution systems is a fascinating research topic in the field of solar energy conversion. A ternary self‐assembled photocatalytic H<jats:sub>2</jats:sub> evolution system was fabricated through supramolecular host–guest chemistry. The system consisted of the H<jats:sub>2</jats:sub> evolution catalyst [Co(dmgH)<jats:sub>2</jats:sub>(4‐ppy)<jats:sub>2</jats:sub>]NO<jats:sub>3</jats:sub> (<jats:bold>1</jats:bold>; dmgH<jats:sub>2</jats:sub>=dimethylglyoxime, 4‐ppy=4‐phenylpyridine) and the photosensitizer Eosin Y (EY) assembled with the macrocyclic compound cucurbit[7]uril (CB[7]) to form the <jats:bold>1</jats:bold>@CB[7]/EY complex through inclusion and exclusion interactions, respectively. The synchronous self‐assembly drives an orthogonal arrangement of the <jats:bold>1</jats:bold>@CB[7]/EY system. The inclusion complex <jats:bold>1</jats:bold>@CB[7] was successfully characterized by <jats:sup>1</jats:sup>H NMR spectroscopy and single‐crystal XRD. The exclusion process of CB[7] with EY was identified by NMR titration and the optimized geometry of the exclusion structure was determined by DFT calculations. The use of CB[7] resulted in a 6‐fold increase in turnover number, a 3‐fold increase in turnover frequency, and a 3‐fold extension of lifetime for photocatalytic H<jats:sub>2</jats:sub> evolution as compared with the system in the absence of CB[7]. The improvement of the light‐driven H<jats:sub>2</jats:sub> evolution activity was ascribed to the ability of CB[7] to link the photosensitizer and catalyst.</jats:p> Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H<sub>2</sub> Evolution ChemSusChem
spellingShingle Song, Dengmeng, Li, Bo, Li, Xin, Sun, Xuzhuo, Li, Jun, Li, Chengbo, Xu, Tongyu, Zhu, Yong, Li, Fei, Wang, Ning, ChemSusChem, Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution, General Energy, General Materials Science, General Chemical Engineering, Environmental Chemistry
title Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_full Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_fullStr Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_full_unstemmed Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_short Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
title_sort orthogonal supramolecular assembly triggered by inclusion and exclusion interactions with cucurbit[7]uril for photocatalytic h<sub>2</sub> evolution
title_unstemmed Orthogonal Supramolecular Assembly Triggered by Inclusion and Exclusion Interactions with Cucurbit[7]uril for Photocatalytic H2 Evolution
topic General Energy, General Materials Science, General Chemical Engineering, Environmental Chemistry
url http://dx.doi.org/10.1002/cssc.201902668